Canonical Allele Identifier: CA1203049841
Gene: NOS1AP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199606G= , CM000663.2:g.162199606G= GRCh38
NC_000001.10:g.162169396G= , CM000663.1:g.162169396G= GRCh37
NC_000001.9:g.160436020G= NCBI36
NG_015979.1:g.134816G=
NG_015979.2:g.134816G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361897.10:c.177+45130G= MANE Select ENSP00000355133.5:n.177+45130G=
ENST00000361897.9:c.177+45130G= ENSP00000355133.5:n.177+45130G=
ENST00000430120.3:c.177+45130G= ENSP00000396713.3:n.177+45130G=
ENST00000530878.5:c.177+45130G= ENSP00000431586.1:n.177+45130G=
NM_001164757.1:c.177+45130G= NP_001158229.1:n.177+45130G=
NM_014697.2:c.177+45130G= NP_055512.1:n.177+45130G=
NM_014697.3:c.177+45130G= MANE Select NP_055512.1:n.177+45130G=
NM_001164757.2:c.177+45130G= NP_001158229.1:n.177+45130G=
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